Source: UNIPROT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs111401431 | 0.763 | 0.200 | 15 | 48468097 | missense variant | G/A | snv | 2 | |||
rs137854464 | 0.851 | 0.200 | 15 | 48425483 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
rs137854480 | 0.742 | 0.200 | 15 | 48537629 | missense variant | G/A | snv | 2 | |||
rs111588631 | 1.000 | 0.160 | 15 | 48428391 | missense variant | A/G | snv | 1 | |||
rs111929350 | 1.000 | 0.160 | 15 | 48452603 | missense variant | C/A;G;T | snv | 1 | |||
rs111984349 | 0.763 | 0.200 | 15 | 48415759 | missense variant | C/T | snv | 1 | |||
rs112375043 | 0.925 | 0.160 | 15 | 48472594 | stop gained | G/A;C;T | snv | 3.6E-05 | 1.4E-05 | 1 | |
rs112660651 | 0.925 | 0.160 | 15 | 48610808 | missense variant | C/A;G;T | snv | 1 | |||
rs112728248 | 0.925 | 0.160 | 15 | 48448812 | missense variant | C/T | snv | 1 | |||
rs112836174 | 0.925 | 0.160 | 15 | 48430791 | missense variant | A/G;T | snv | 1 | |||
rs113544411 | 0.925 | 0.160 | 15 | 48421652 | stop gained | G/A;C;T | snv | 1.2E-05 | 1 | ||
rs137854456 | 0.925 | 0.160 | 15 | 48487365 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-05 | 1 | ||
rs137854457 | 0.925 | 0.160 | 15 | 48428423 | missense variant | C/G;T | snv | 1 | |||
rs137854458 | 1.000 | 0.160 | 15 | 48483910 | missense variant | C/G | snv | 1 | |||
rs137854459 | 1.000 | 0.160 | 15 | 48463977 | missense variant | A/G | snv | 1 | |||
rs137854460 | 0.925 | 0.160 | 15 | 48432943 | missense variant | C/G;T | snv | 1 | |||
rs137854461 | 0.790 | 0.280 | 15 | 48437026 | missense variant | T/C | snv | 1 | |||
rs137854462 | 1.000 | 0.160 | 15 | 48510115 | missense variant | T/A | snv | 1 | |||
rs137854463 | 1.000 | 0.160 | 15 | 48497391 | missense variant | T/G | snv | 1 | |||
rs137854465 | 0.925 | 0.160 | 15 | 48488230 | missense variant | A/G | snv | 1 | |||
rs137854467 | 0.790 | 0.280 | 15 | 48600217 | missense variant | G/A | snv | 1 | |||
rs137854468 | 0.851 | 0.160 | 15 | 48487396 | missense variant | C/T | snv | 1 | |||
rs137854469 | 1.000 | 0.160 | 15 | 48485418 | missense variant | C/A;T | snv | 1 | |||
rs137854470 | 1.000 | 0.160 | 15 | 48487425 | missense variant | C/T | snv | 1 | |||
rs137854471 | 0.925 | 0.160 | 15 | 48483931 | missense variant | C/T | snv | 1 |